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BMC Pediatr ; 24(1): 408, 2024 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-38918745

RESUMEN

Hypereosinophilia is a rare presentation in all age groups, particularly when it is severe, persistent, and progressive. We describe the clinical characteristics and course of severe hypereosinophilia in a full-term Saudi female neonate. A febrile respiratory illness evolved with a progressive increase in peripheral blood leukocyte and eosinophil counts, reaching 44.9% of leukocytes and an absolute value of 57,000 cells/µl. Different etiological examinations (for viral, bacterial, immunodeficiency, hyper IgE syndrome, gene mutations) revealed extremely high CMV antigenemia and a homozygous mutation in the STAT1 gene. Anhelation was relieved by oxygen and anti-viral treatment. Steroids brought a dramatic response in peripheral blood counts within 24 h. After a 6-week course of antiviral and steroid treatment at home, she had an excellent general condition. Conclusion: Although a rare pathology, it is important to consider genetic disorders when there is an atypical immune response to viral infections.


Asunto(s)
Infecciones por Citomegalovirus , Mutación , Factor de Transcripción STAT1 , Humanos , Femenino , Factor de Transcripción STAT1/genética , Recién Nacido , Infecciones por Citomegalovirus/complicaciones , Eosinofilia/genética
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